Non-steady catalytic performance as a tool for the identification of the active surface in VPO, catalyst for n-butane oxidation to maleic anhydride

被引:28
作者
Ballarini, N.
Cavani, F.
Cortelli, C.
Ricotta, M.
Rodeghiero, F.
Trifiro, F.
Fumagalli, C.
Mazzoni, G.
机构
[1] Univ Bologna, Dipartimento Chim Ind & Mat, I-40136 Bologna, Italy
[2] INSTM, Res Unit Bologna, Bologna, Italy
[3] Lonza SpA, I-24020 Scanzorosciate, BG, Italy
关键词
vanadyl pyrophosphate; maleic anhydride; n-butane oxidation; vanadium phosphate;
D O I
10.1016/j.cattod.2006.05.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The reactivity of equilibrated VPO catalysts with different P/V ratio was investigated under steady and unsteady conditions, with the aim of gaining information on the status of the active surface in reaction conditions. Specific treatments were applied, and then the unsteady performance was followed along with the reaction time, until the steady behaviour was recovered. These transient states made possible to infer that the nature of the true active surface is a function of the VPO characteristics and of the reaction conditions. With the catalyst having P/V ratio >1.0, the hydrolysis of the VPP surface under working conditions at temperatures higher than 340-350 degrees C, followed by the oxidation of vanadium, generates an active layer made of vanadium oxide and of P2O5/H2O. When instead the P/V ratio is close to 1.0, the VPP surface is oxidized to VOPO4 already at mild temperature under working conditions, with development of an active layer which is very active but unselective to maleic anhydride at 380 degrees C. Higher temperatures then lead to the hydrolysis of VOPO4, with generation of an active layer which is similar, and behaves similarly, to that one which develops with the catalyst having P/V ratio >1.0. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:174 / 179
页数:6
相关论文
共 29 条
[1]   A MOLECULAR-LEVEL MECHANISM OF N-BUTANE OXIDATION TO MALEIC-ANHYDRIDE OVER VANADYL PYROPHOSPHATE [J].
AGASKAR, PA ;
DECAUL, L ;
GRASSELLI, RK .
CATALYSIS LETTERS, 1994, 23 (3-4) :339-351
[2]   REDOX INTERACTION OF AMMONIA WITH (VO)(2)P2O7 [J].
BERNDT, H ;
BUKER, K ;
MARTIN, A ;
BRUCKNER, A ;
LUCKE, B .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (04) :725-731
[3]   In situ surface analysis in selective oxidation catalysis:: n-butane conversion over VPP [J].
Bluhm, H ;
Hävecker, M ;
Kleimenov, E ;
Knop-Gericke, A ;
Liskowski, A ;
Schlögl, R ;
Su, DS .
TOPICS IN CATALYSIS, 2003, 23 (1-4) :99-107
[4]   Synergistic effects in selective oxidation catalysis: does phase cooperation result in site isolation? [J].
Bordes, E .
TOPICS IN CATALYSIS, 2001, 15 (2-4) :131-137
[5]   The role of structural chemistry of selective catalysts in heterogeneous mild oxidation of hydrocarbons [J].
Bordes, E .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE, 2000, 3 (09) :725-733
[6]   Investigation of vanadium phosphorus oxide catalysts (VPO) during toluene ammoxidation: New mechanistic insights by in situ EPR [J].
Bruckner, A ;
Martin, A ;
Steinfeldt, N ;
Wolf, GU ;
Lucke, B .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (21) :4257-4263
[7]   In situ electron spin resonance: A useful tool for the investigation of vanadium phosphate catalysts (VPO) under working conditions [J].
Bruckner, A ;
Kubias, B ;
Lucke, B .
CATALYSIS TODAY, 1996, 32 (1-4) :215-222
[8]   Structure of vanadium sites in VPO catalysts and their influence on the catalytic performance in selective O- and N-insertion reactions [J].
Bruckner, A ;
Martin, A ;
Kubias, B ;
Lucke, B .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1998, 94 (15) :2221-2225
[9]  
CAVANI F, 1985, APPL CATAL, V15, P151, DOI 10.1016/S0166-9834(00)81495-5
[10]  
Cavani F., 1994, CATALYSIS, V11, P246